|
661
|
|
|
Anoctamin 2 |
C12orf3, TMEM16B |
|
|
662
|
|
|
AarF domain containing kinase 1 |
MCP2 |
|
|
663
|
|
|
ADAMTS like 3 |
ADAMTSL-3 |
|
|
664
|
|
|
ATPase phospholipid transporting 10A (putative) |
ATP10C, ATPVA, ATPVC |
|
|
665
|
|
|
ATPase phospholipid transporting 8B2 |
ATPID |
|
|
666
|
|
|
Adhesion G protein-coupled receptor G6 |
APG1, DREG, GPR126, LCCS9, PR126, PS1TP2, VIGR |
|
|
667
|
|
|
Activation induced cytidine deaminase |
AID, ARP2, CDA2, HEL-S-284, HIGM2 |
|
|
668
|
|
|
Arsenite methyltransferase |
CYT19 |
Anxiety disorder, Arsenic encephalopathy, Attention deficit hyperactivity disorder, Bipolar disorder, Urinary bladder cancer, Bladder neoplasm, Neoplasm, Coronary artery disease, Development disorder, Epithelioma, Glandular neoplasms, Mental depression, Minimal brain dysfunction, Schizophrenia |
|
669
|
|
|
Aryl hydrocarbon receptor repressor |
AHH, AHHR, bHLHe77 |
|
|
670
|
|
|
AT-rich interaction domain 1B |
6A3-5, BAF250B, BRIGHT, CSS1, DAN15, ELD/OSA1, MRD12, OSA2, P250R, SMARCF2 |
6q24-q25 deletion syndrome, 6q25 microdeletion syndrome, Agenesis of corpus callosum, Anonychia, Astigmatism, Atrial septal defect, Autism, Blepharophimosis, Brachycephaly, Breast adenocarcinoma, Breast cancer, Breast carcinoma, Camptodactyly of fingers, Cataract, Choanal atresia, Coffin-siris syndrome, Colpocephaly, Congenital diaphragmatic hernia, Congenital megaureter, Dislocated radial head, Congenital epicanthus, Congenital exomphalos, Congenital malrotation of intestine, Congenital talipes calcaneovalgus, Cryptorchidism, Cutis marmorata, Dandy-walker syndrome, Developmental delay, Duodenal ulcer, Dwarfism, Dysautonomia, Dysmorphic features, Dysphagia, Ectopic kidney, Eczema, Epilepsy, Esotropia, Expressive language delay, Frontal bossing, Gastric ulcer, Hearing loss, Hemangioma, High palate, Hirschsprung disease, Hydronephrosis, Hyperkeratosis pilaris, Hypertrichosis, Hypoplasia of corpus callosum, Hypospadias, Hypothyroidism, Intussusception, Laryngomalacia, Liver carcinoma, Macrocephaly, Macrostomia, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Movement disorders, Multiple congenital anomalies, Myopia, Nail dysplasia, Hypotonia, Neuroblastoma, Neurodevelopmental disorders, Nicolaides baraitser syndrome, Nystagmus, Partial agenesis of corpus callosum, Patent ductus arteriosus, Plagiocephaly, Posteriorly rotated ear, Ptosis, Renal hypoplasia, Scoliosis, Speech disorders, Spina bifida occulta, Strabismus, Strawberry nevus of skin, Tetralogy of fallot, Ventricular septal defect, Vertical talus, Vesicoureteral refluxView all (69 more) |
